Detailed Information on Publication Record
2021
SiO2-Decorated Parylene C Micropillars Designed to Probe Cellular Force
FOHLEROVÁ, Zdenka, Imrich GABLECH, Alexandr OTAHAL and Peter FECKOBasic information
Original name
SiO2-Decorated Parylene C Micropillars Designed to Probe Cellular Force
Authors
FOHLEROVÁ, Zdenka (203 Czech Republic, guarantor, belonging to the institution), Imrich GABLECH (203 Czech Republic), Alexandr OTAHAL (203 Czech Republic) and Peter FECKO (703 Slovakia)
Edition
ADVANCED MATERIALS INTERFACES, HOBOKEN, WILEY, 2021, 2196-7350
Other information
Language
English
Type of outcome
Článek v odborném periodiku
Field of Study
10404 Polymer science
Country of publisher
United States of America
Confidentiality degree
není předmětem státního či obchodního tajemství
References:
Impact factor
Impact factor: 6.389
RIV identification code
RIV/00216224:14110/21:00121732
Organization unit
Faculty of Medicine
UT WoS
000611098000001
Keywords in English
cellular force; mechanobiology; micropillars; parylene C; silanization; silicon dioxide
Tags
International impact, Reviewed
Změněno: 8/6/2021 13:00, Mgr. Tereza Miškechová
Abstract
V originále
Living cells sense and respond to mechanical signals through specific mechanisms generating traction force. The quantification of cell forces using micropillars can be limited by micropillar stiffness, technological aspects of fabrications, and microcontact printing of proteins. This paper develops the new design of SiO2/Parylene C micropillars with an aspect ratio of 6 and 3.5 and spring constant of 4.7 and 28 mu N mu m(-1), respectively. The upper part of micropillars is coated with a 250 nm layer of SiO2, and results confirm protein deposition on individual micropillars via SiO2 interface and non-adhesiveness on the micropillars' sidewalls. Results show an absence of cytotoxicity for micropillar-based substrates and a dependence on its stiffness. Stiffer micropillars enhance cell adhesion and proliferation rate, and a stronger cellular force of approximate to 25 mu N is obtained. The main contribution of SiO2/parylene C micropillars is the elimination of the step involving the fabrication of polydimethylsiloxane stamp because the array enables covalent binding of proteins via SiO2 chemistry. These micropillars stand on Si wafer and thus, any warping of underlying polymer membrane does not have to be considered. Additionally, SiO2/parylene C micropillars can broaden the range of stiffer substrates to be probed by cells.